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Refined by: Journal Title: Journal Of Organic Chemistry remove
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1
A β-Keto Ester as a Novel, Efficient, and Versatile Ligand for Copper(I)-Catalyzed C−N, C−O, and C−S Coupling Reactions
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A β-Keto Ester as a Novel, Efficient, and Versatile Ligand for Copper(I)-Catalyzed C−N, C−O, and C−S Coupling Reactions

Journal of organic chemistry, 2007-05, Vol.72 (10), p.3863-3867 [Peer Reviewed Journal]

Copyright © 2007 American Chemical Society ;2007 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo070443m ;PMID: 17432916 ;CODEN: JOCEAH

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2
Mechanistic Studies on the Cu-Catalyzed Three-Component Reactions of Sulfonyl Azides, 1-Alkynes and Amines, Alcohols, or Water: Dichotomy via a Common Pathway
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Mechanistic Studies on the Cu-Catalyzed Three-Component Reactions of Sulfonyl Azides, 1-Alkynes and Amines, Alcohols, or Water: Dichotomy via a Common Pathway

Journal of organic chemistry, 2008-07, Vol.73 (14), p.5520-5528 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-3263 ;ISSN: 1520-6904 ;EISSN: 1520-6904 ;DOI: 10.1021/jo800733p ;PMID: 18557650 ;CODEN: JOCEAH

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3
Palladium-Catalyzed Carbonylation Reactions of Aryl Bromides at Atmospheric Pressure: A General System Based on Xantphos
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Palladium-Catalyzed Carbonylation Reactions of Aryl Bromides at Atmospheric Pressure: A General System Based on Xantphos

Journal of organic chemistry, 2008-09, Vol.73 (18), p.7102-7107 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo801279r ;PMID: 18720970 ;CODEN: JOCEAH

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4
Zinc(II) Perchlorate Hexahydrate Catalyzed Opening of Epoxide Ring by Amines:  Applications to Synthesis of (RS)/(R)-Propranolols and (RS)/(R)/(S)-Naftopidils
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Zinc(II) Perchlorate Hexahydrate Catalyzed Opening of Epoxide Ring by Amines:  Applications to Synthesis of (RS)/(R)-Propranolols and (RS)/(R)/(S)-Naftopidils

Journal of organic chemistry, 2007-05, Vol.72 (10), p.3713-3722 [Peer Reviewed Journal]

Copyright © 2007 American Chemical Society ;2007 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo062674j ;PMID: 17411096 ;CODEN: JOCEAH

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5
Epi-Cinchona Based Thiourea Organocatalyst Family as an Efficient Asymmetric Michael Addition Promoter: Enantioselective Conjugate Addition of Nitroalkanes to Chalcones and α,β-Unsaturated N-Acylpyrroles
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Epi-Cinchona Based Thiourea Organocatalyst Family as an Efficient Asymmetric Michael Addition Promoter: Enantioselective Conjugate Addition of Nitroalkanes to Chalcones and α,β-Unsaturated N-Acylpyrroles

Journal of organic chemistry, 2008-05, Vol.73 (9), p.3475-3480 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo702692a ;PMID: 18376862 ;CODEN: JOCEAH

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6
Nucleophilic Fluoroalkylation of α,β-Enones, Arynes, and Activated Alkynes with Fluorinated Sulfones: Probing the Hard/Soft Nature of Fluorinated Carbanions
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Nucleophilic Fluoroalkylation of α,β-Enones, Arynes, and Activated Alkynes with Fluorinated Sulfones: Probing the Hard/Soft Nature of Fluorinated Carbanions

Journal of organic chemistry, 2008-08, Vol.73 (15), p.5699-5713 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo702479z ;PMID: 18593187 ;CODEN: JOCEAH

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7
CF3 Oxonium Salts, O-(Trifluoromethyl)dibenzofuranium Salts:  In Situ Synthesis, Properties, and Application as a Real CF3 + Species Reagent
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CF3 Oxonium Salts, O-(Trifluoromethyl)dibenzofuranium Salts:  In Situ Synthesis, Properties, and Application as a Real CF3 + Species Reagent

Journal of organic chemistry, 2007-08, Vol.72 (18), p.6905-6917 [Peer Reviewed Journal]

Copyright © 2007 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo070896r ;PMID: 17676906 ;CODEN: JOCEAH

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8
Metal Triflate-Catalyzed Cationic Benzylation and Allylation of 1,3-Dicarbonyl Compounds
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Metal Triflate-Catalyzed Cationic Benzylation and Allylation of 1,3-Dicarbonyl Compounds

Journal of organic chemistry, 2007-07, Vol.72 (14), p.5161-5167 [Peer Reviewed Journal]

Copyright © 2007 American Chemical Society ;2007 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo0705216 ;PMID: 17555355 ;CODEN: JOCEAH

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9
One-Step Synthesis of Heterocyclic Privileged Medicinal Scaffolds by a Multicomponent Reaction of Malononitrile with Aldehydes and Thiols
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One-Step Synthesis of Heterocyclic Privileged Medicinal Scaffolds by a Multicomponent Reaction of Malononitrile with Aldehydes and Thiols

Journal of organic chemistry, 2007-04, Vol.72 (9), p.3443-3453 [Peer Reviewed Journal]

Copyright © 2007 American Chemical Society ;2007 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo070114u ;PMID: 17408286 ;CODEN: JOCEAH

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10
Supramolecular Analytical Chemistry
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Supramolecular Analytical Chemistry

Journal of organic chemistry, 2007-02, Vol.72 (3), p.687-699 [Peer Reviewed Journal]

Copyright © 2007 American Chemical Society ;2007 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo0617971 ;PMID: 17253783 ;CODEN: JOCEAH

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11
Divalent Lanthanide Complexes: Highly Active Precatalysts for the Addition of N−H and C−H Bonds to Carbodiimides
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Divalent Lanthanide Complexes: Highly Active Precatalysts for the Addition of N−H and C−H Bonds to Carbodiimides

Journal of organic chemistry, 2008-11, Vol.73 (22), p.8966-8972 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;2009 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo801693z ;PMID: 18937411 ;CODEN: JOCEAH

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12
Parallel Synthesis of a Library of Benzoxazoles and Benzothiazoles Using Ligand-Accelerated Copper-Catalyzed Cyclizations of ortho-Halobenzanilides
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Parallel Synthesis of a Library of Benzoxazoles and Benzothiazoles Using Ligand-Accelerated Copper-Catalyzed Cyclizations of ortho-Halobenzanilides

Journal of organic chemistry, 2006-03, Vol.71 (5), p.1802-1808 [Peer Reviewed Journal]

Copyright © 2006 American Chemical Society ;2007 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo051927q ;PMID: 16496964 ;CODEN: JOCEAH

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13
Highly Enantioselective Henry (Nitroaldol) Reaction of Aldehydes and α-Ketoesters Catalyzed by N,N‘-Dioxide-Copper(I) Complexes
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Highly Enantioselective Henry (Nitroaldol) Reaction of Aldehydes and α-Ketoesters Catalyzed by N,N‘-Dioxide-Copper(I) Complexes

Journal of organic chemistry, 2007-11, Vol.72 (24), p.9323-9328 [Peer Reviewed Journal]

Copyright © 2007 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo701898r ;PMID: 17973533 ;CODEN: JOCEAH

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14
Reusable Cu2O/PPh3/TBAB System for the Cross-Couplings of Aryl Halides and Heteroaryl Halides with Terminal Alkynes
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Reusable Cu2O/PPh3/TBAB System for the Cross-Couplings of Aryl Halides and Heteroaryl Halides with Terminal Alkynes

Journal of organic chemistry, 2007-08, Vol.72 (16), p.6294-6297 [Peer Reviewed Journal]

Copyright © 2007 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo070538o ;PMID: 17616146 ;CODEN: JOCEAH

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15
The Direct Organocatalytic Asymmetric Mannich Reaction:  Unmodified Aldehydes as Nucleophiles
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The Direct Organocatalytic Asymmetric Mannich Reaction:  Unmodified Aldehydes as Nucleophiles

Journal of organic chemistry, 2003-12, Vol.68 (25), p.9624-9634 [Peer Reviewed Journal]

Copyright © 2003 American Chemical Society ;2004 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo0347359 ;PMID: 14656087 ;CODEN: JOCEAH

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16
Facile Nucleophilic Fluorination Reactions Using tert-Alcohols as a Reaction Medium:  Significantly Enhanced Reactivity of Alkali Metal Fluorides and Improved Selectivity
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Facile Nucleophilic Fluorination Reactions Using tert-Alcohols as a Reaction Medium:  Significantly Enhanced Reactivity of Alkali Metal Fluorides and Improved Selectivity

Journal of organic chemistry, 2008-02, Vol.73 (3), p.957-962 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo7021229 ;PMID: 18166063 ;CODEN: JOCEAH

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17
Solid-phase approaches for labelling targeting peptides with far-red emitting coumarin fluorophores
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Solid-phase approaches for labelling targeting peptides with far-red emitting coumarin fluorophores

Journal of organic chemistry, 2019-02 [Peer Reviewed Journal]

(c) American Chemical Society , 2019 info:eu-repo/semantics/openAccess ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/acs.joc.8b02624

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18
Phosphine-Free Cross-Coupling Reaction of Arylboronic Acids with Carboxylic Anhydrides or Acyl Chlorides in Aqueous Media
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Phosphine-Free Cross-Coupling Reaction of Arylboronic Acids with Carboxylic Anhydrides or Acyl Chlorides in Aqueous Media

Journal of organic chemistry, 2006-07, Vol.71 (15), p.5725-5731 [Peer Reviewed Journal]

Copyright © 2006 American Chemical Society ;2007 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo060749d ;PMID: 16839154 ;CODEN: JOCEAH

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19
Lessons from Nature: Biomimetic Organocatalytic Carbon−Carbon Bond Formations
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Lessons from Nature: Biomimetic Organocatalytic Carbon−Carbon Bond Formations

Journal of organic chemistry, 2008-10, Vol.73 (20), p.7857-7870 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo801374j ;PMID: 18778100 ;CODEN: JOCEAH

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20
Ligand-Free Copper-Catalyzed C−S Coupling of Aryl Iodides and Thiols
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Ligand-Free Copper-Catalyzed C−S Coupling of Aryl Iodides and Thiols

Journal of organic chemistry, 2008-07, Vol.73 (14), p.5625-5628 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;2008 INIST-CNRS ;ISSN: 0022-3263 ;EISSN: 1520-6904 ;DOI: 10.1021/jo800491k ;PMID: 18570479 ;CODEN: JOCEAH

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